Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2377192T>C , CM000673.2:g.2377192T>C | GRCh38 |
| NC_000011.9:g.2398422T>C , CM000673.1:g.2398422T>C | GRCh37 |
| NC_000011.8:g.2354998T>C | NCBI36 |
| NG_023386.1:g.4876T>C , LRG_142:g.4876T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001297649.1:c.-148+835T>C (CD81) | NP_001284578.1:n.-148+835T>C |
| NM_001297649.2:c.-148+835T>C (CD81) | NP_001284578.1:n.-148+835T>C |
| NR_108080.1:n.407+394A>G (CD81-AS1) | |
| ENST00000475945.6:c.-148+835T>C (CD81) | ENSP00000433178.1:n.-148+835T>C |
| ENST00000475945.7:c.-148+835T>C (CD81) | ENSP00000433178.2:n.-148+835T>C |
| ENST00000530648.5:c.-148+272T>C (CD81) | ENSP00000432723.1:n.-148+272T>C |